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rs878853374

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853374(C;T)
Make rs878853374(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position38304761
GeneRPGR
is asnp
is mentioned by
dbSNPrs878853374
ebirs878853374
HLIrs878853374
Exacrs878853374
Varsomers878853374
Maprs878853374
PheGenIrs878853374
hapmaprs878853374
1000 genomesrs878853374
hgdprs878853374
ensemblrs878853374
gopubmedrs878853374
geneviewrs878853374
scholarrs878853374
googlers878853374
pharmgkbrs878853374
gwascentralrs878853374
openSNPrs878853374
23andMers878853374
23andMe allrs878853374
SNP Nexus

SNPshotrs878853374
SNPdbers878853374
MSV3drs878853374
GWAS Ctlgrs878853374
Max Magnitude0
ClinVar
Risk rs878853374(T;T)
Alt rs878853374(T;T)
Reference rs878853374(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RPGR
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000023.10:g.38164014G>A
CLNSRC
CLNACC RCV000225612.1,